Canonical Allele Identifier: CA1737037502

Gene: MET

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.116771744T= , CM000669.2:g.116771744T=	GRCh38
NC_000007.13:g.116411798T= , CM000669.1:g.116411798T=	GRCh37
NC_000007.12:g.116199034T=	NCBI36
NG_008996.1:g.104340T= , LRG_662:g.104340T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436117.3:c.*492+90T=	ENSP00000410980.2:n.*492+90T=
ENST00000318493.11:c.2941+90T=	ENSP00000317272.6:n.2941+90T=
ENST00000397752.8:c.2887+90T= MANE Select	ENSP00000380860.3:n.2887+90T=
ENST00000318493.10:c.2941+90T=	ENSP00000317272.6:n.2941+90T=
ENST00000397752.7:c.2887+90T=	ENSP00000380860.3:n.2887+90T=
ENST00000454623.1:c.283+90T=	ENSP00000398140.1:n.283+90T=
NM_000245.2:c.2887+90T=	NP_000236.2:n.2887+90T=
NM_001127500.1:c.2941+90T= , LRG_662t1:c.2941+90T=	NP_001120972.1:n.2941+90T=
XM_006715990.2:c.1597+90T=	XP_006716053.1:n.1597+90T=
XM_006715991.2:c.1597+90T=	XP_006716054.1:n.1597+90T=
XM_011516223.1:c.2944+90T=	XP_011514525.1:n.2944+90T=
NM_000245.3:c.2887+90T=	NP_000236.2:n.2887+90T=
NM_001127500.2:c.2941+90T=	NP_001120972.1:n.2941+90T=
NM_001324402.1:c.1597+90T=	NP_001311331.1:n.1597+90T=
XR_001744772.1:n.3018+90T=
NM_001127500.3:c.2941+90T=	NP_001120972.1:n.2941+90T=
NM_000245.4:c.2887+90T= MANE Select	NP_000236.2:n.2887+90T=
NM_001324402.2:c.1597+90T=	NP_001311331.1:n.1597+90T=